Zheng Peng-Fei, Yin Rui-Xing, Cao Xiao-Li, Guan Yao-Zong, Deng Guo-Xiong, Wei Bi-Liu, Liu Chun-Xiao
Department of Cardiology, Institute of Cardiovascular Diseases, The First Affiliated Hospital, Guangxi Medical University, Nanning, China.
Guangxi Key Laboratory Base of Precision Medicine in Cardio-Cerebrovascular Disease Control and Prevention, Nanning, China.
Front Genet. 2021 Jul 21;12:679027. doi: 10.3389/fgene.2021.679027. eCollection 2021.
The current study aims to further delineate the associations between the synaptotagmin-like 3 () and solute carrier family 22 member 3 () single-nucleotide polymorphisms (SNPs) and their haplotypes and gene-gene (G × G)/environment (G × E) interactions on the risk of hyperlipidemia (HLP) in the Maonan and Han ethnic groups. Genotype distribution among the SNPs in 2,829 individual patients bearing no relationship to each other (Han, 1,436; Maonan, 1,393) was analyzed utilizing next-generation sequencing techniques. The genotype frequencies of the rs6455600, rs2129209, and rs446809 SNPs were varied between the two ethnic groups ( < 0.05-0.001). Various SNPs were correlated with serum levels of triglyceride (TG; rs446809), total cholesterol (TC; rs6455600, rs2129209, and rs539298), and low-density lipoprotein cholesterol (LDL-C; rs446809) among the Han population, whereas various SNPs were also correlated with TC (rs6455600 and rs539298), TG (rs446809), and LDL-C (rs446809) levels in the Maonan ethnic group ( < 0.008-0.001). One part of haplotypes resulted in worsened HLP-related morbidity in the Han ( A-C-A-A; A-A and A-G; and A-C-A-A-A-A and A-C-A-A-A-G) and Maonan ( A-C-A-A; A-A and A-G; and A-C-A-A-A-A, G-T-C-A-A-A, and G-T-C-A-C-A) ethnic groups, whereas another part of haplotypes lowered HLP-related health risks in the Han ( C-A and C-G and A-C-A-A-C-A, A-C-A-A-C-G, and G-T-C-A-C-A) and Maonan ( C-G and A-C-A-A-C-G) ethnic groups. We discovered that the SNPs and their haplotypes were associated with serum lipid levels and the risk of HLP in our studied populations.
本研究旨在进一步阐明毛南族和汉族中,类突触结合蛋白样3()和溶质载体家族22成员3()单核苷酸多态性(SNPs)及其单倍型与基因-基因(G×G)/环境(G×E)相互作用对高脂血症(HLP)风险的影响。利用下一代测序技术分析了2829例无亲缘关系个体患者(汉族1436例,毛南族1393例)中这些SNPs的基因型分布。rs6455600、rs2129209和rs446809 SNPs的基因型频率在两个民族之间存在差异(<0.05-0.001)。汉族人群中,不同的SNPs与甘油三酯(TG;rs446809)、总胆固醇(TC;rs6455600、rs2129209和rs539298)以及低密度脂蛋白胆固醇(LDL-C;rs446809)的血清水平相关;而在毛南族中,不同的SNPs也与TC(rs6455600和rs539298)、TG(rs446809)以及LDL-C(rs446809)水平相关(<0.008-0.001)。一部分单倍型导致汉族(A-C-A-A;A-A和A-G;以及A-C-A-A-A-A和A-C-A-A-A-G)和毛南族(A-C-A-A;A-A和A-G;以及A-C-A-A-A-A、G-T-C-A-A-A和G-T-C-A-C-A)人群中与HLP相关的发病率升高,而另一部分单倍型则降低了汉族(C-A和C-G以及A-C-A-A-C-A、A-C-A-A-C-G和G-T-C-A-C-A)和毛南族(C-G以及A-C-A-A-C-G)人群中与HLP相关的健康风险。我们发现,这些SNPs及其单倍型与我们研究人群中的血脂水平和HLP风险相关。